Skip to main content

Preoperative and Intraoperative Lymphatic Mapping for Radioguided Sentinel Node Biopsy in Cancers of the Female Reproductive System

  • Chapter
  • First Online:
Atlas of Lymphoscintigraphy and Sentinel Node Mapping

Abstract

Sentinel lymph node is the first lymph node with direct lymphatic drainage from the primary tumor, so it can predict the overall lymph node status. Sentinel lymph node biopsy is recommended as the standard of care for well-selected women with early-stage vulvar cancer (stages IB and II), cervical cancer (stage IA1 with lymphovascular invasion, stages IA2, IB1, and IIA1), and endometrial cancer (stages IB and II). The combination of radiotracer and blue dye is nowadays the most appropriate technique for sentinel lymph node mapping, especially for cervical cancer. There is a growing interest for hybrid tracer known as indocyanine green-99mTc-nanocolloid in vulvar cancer and cervical cancer. SPECT/CT imaging enables to personalize lymphatic mapping, providing detailed information about the number and anatomical location of sentinel lymph nodes for adequate surgical planning. Sentinel lymph node biopsy in patients with cancers of the female reproductive system should be performed in experienced, tertiary referral centers.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 79.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 99.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 139.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Giammarile F, Bozkurt MF, Cibula D, et al. The EANM clinical and technical guidelines for lymphoscintigraphy and sentinel node localization in gynaecological cancers. Eur J Nucl Med Mol Imaging. 2014;41(7):1463–77.

    Google Scholar 

  2. Koh WJ, Abu-Rustum NR, Bean S, et al. NCCN clinical practice guidelines in oncology (NCCN guidelines), vulvar cancer (squamous cell carcinoma): version 2.2019. 2018. https://www.nccn.org/professionals/physician_gls/pdf/vulvar.pdf. Accessed 6 Aug 2019.

  3. Oonk MHM, Planchamp F, Baldwin P, et al. European Society of Gynaecological Oncology guidelines for the management of patients with vulvar cancer. Int J Gynecol Cancer. 2017;27(4):832–7.

    Article  Google Scholar 

  4. Koh WJ, Abu-Rustum NR, Bean S, et al. Cervical cancer, version 3.2019, NCCN clinical practice guidelines in oncology. J Natl Compr Cancer Netw. 2019;17(1):64–84.

    Google Scholar 

  5. Koh WJ, Abu-Rustum NR, Bean S, et al. NCCN clinical practice guidelines in oncology (NCCN guidelines), uterine neoplasms: version 3.2019. 2019. https://www.nccn.org/professionals/physician_gls/pdf/uterine.pdf. Accessed 6 Aug 2019.

  6. Levenback C, Burke TW, Gershenson DM, et al. Intraoperative lymphatic mapping for vulvar cancer. Obstet Gynecol. 1994;84(2):163–7.

    Google Scholar 

  7. Burke TW, Levenback C, Tornos C, et al. Intra-abdominal lymphatic mapping to direct selective pelvic and paraaortic lymphadenectomy in women with high-risk endometrial cancer: results of a pilot study. Gynecol Oncol. 1996;62(2):169–73.

    Google Scholar 

  8. Levenback C, Coleman RL, Burke TW, et al. Lymphatic mapping and sentinel node identification in patients with cervix cancer undergoing radical hysterectomy and pelvic lymphadenectomy. J Clin Oncol. 2002;20:688–93.

    Google Scholar 

  9. Van der Zee AG, Oonk MH, De Hullu JA, et al. Sentinel node dissection is safe in the treatment of early-stage vulvar cancer. J Clin Oncol. 2008;26(6):884–9.

    Google Scholar 

  10. Lécuru F, Mathevet P, Querleu D, et al. Bilateral negative sentinel nodes accurately predict absence of lymph node metastasis in early cervical cancer: results of the SENTICOL study. J Clin Oncol. 2011;29(13):1686–91.

    Google Scholar 

  11. Crane LM, Themelis G, Arts HJ, et al. Intraoperative near-infrared fluorescence imaging for sentinel lymph node detection in vulvar cancer: first clinical results. Gynecol Oncol. 2011;120(2):291–5.

    Google Scholar 

  12. Rossi EC, Ivanova A, Boggess JF. Robotically assisted fluorescence-guided lymph node mapping with ICG for gynecologic malignancies: a feasibility study. Gynecol Oncol. 2012;124(1):78–82.

    Article  Google Scholar 

  13. Mathéron HM, van den Berg NS, Brouwer OR, et al. Multimodal surgical guidance towards the sentinel node in vulvar cancer. Gynecol Oncol. 2013;131(3):720–5.

    Google Scholar 

  14. Verbeek FP, Tummers QR, Rietbergen DD, et al. Sentinel lymph node biopsy in vulvar cancer using combined radioactive and fluorescence guidance. Int J Gynecol Cancer. 2015;25(6):1086–93.

    Google Scholar 

  15. Paredes P, Vidal-Sicart S, Campos F, et al. Role of ICG-99mTc-nanocolloid for sentinel lymph node detection in cervical cancer: a pilot study. Eur J Nucl Med Mol Imaging. 2017;44(11):1853–61.

    Google Scholar 

  16. Howlader N, Noone AM, Krapcho M, et al. SEER cancer statistics review, 1975–2014. Bethesda: National Cancer Institute; 2017. https://seer.cancer.gov/csr/1975_2014/, based on November 2016 SEER data submission, posted to the SEER web site, April 2017.

  17. Del Pino M, Rodriguez-Carunchio L, Ordi J. Pathways of vulvar intraepithelial neoplasia and squamous cell carcinoma. Histopathology. 2013;62(1):161–75.

    Article  Google Scholar 

  18. Hacker NF, Eifel PJ, van der Velden J. Cancer of the vulva. Int J Gynaecol Obstet. 2012;119(2):S90–6.

    Article  Google Scholar 

  19. Burger MP, Hollema H, Emanuels AG, et al. The importance of the groin node status for the survival of T1 and T2 vulval carcinoma patients. Gynecol Oncol. 1995;57(3):327–34.

    Google Scholar 

  20. Gaarenstroom KN, Kenter GG, Trimbos JB, et al. Postoperative complications after vulvectomy and inguinofemoral lymphadenectomy using separate groin incisions. Int J Gynecol Cancer. 2003;13(4):522–7.

    Google Scholar 

  21. Te Grootenhuis NC, van der Zee AG, van Doorn HC, et al. Sentinel nodes in vulvar cancer: long-term follow-up of the GROningen INternational study on sentinel nodes in vulvar cancer (GROINSS-V) I. Gynecol Oncol. 2016;140(1):8–14.

    Google Scholar 

  22. McCann GA, Cohn DE, Jewell EL, et al. Lymphatic mapping and sentinel lymph node dissection compared to complete lymphadenectomy in the management of early-stage vulvar cancer: a cost-utility analysis. Gynecol Oncol. 2015;136(2):300–4.

    Google Scholar 

  23. Kim SM, Choi HS, Byun JS. Overall 5-year survival rate and prognostic factors in patients with stage IB and IIA cervical cancer treated by radical hysterectomy and pelvic lymph node dissection. Int J Gynecol Cancer. 2000;10(4):305–12.

    Article  Google Scholar 

  24. Benedetti-Panici P, Maneschi F, Scambia G, et al. Lymphatic spread of cervical cancer: an anatomical and pathological study based on 225 radical hysterectomies with systematic pelvic and aortic lymphadenectomy. Gynecol Oncol. 1996;62(1):19–24.

    Google Scholar 

  25. Bats AS, Mathevet P, Buenerd A, et al. The sentinel node technique detects unexpected drainage pathways and allows nodal ultrastaging in early cervical cancer: insights from the multicenter prospective SENTICOL study. Ann Surg Oncol. 2013;20(2):413–22.

    Google Scholar 

  26. Marnitz S, Köhler C, Bongardt S, et al. Topographic distribution of sentinel lymph nodes in patients with cervical cancer. Gynecol Oncol. 2006;103(1):35–44.

    Google Scholar 

  27. Cormier B, Diaz JP, Shih K, et al. Establishing a sentinel lymph node mapping algorithm for the treatment of early cervical cancer. Gynecol Oncol. 2011;122(2):275–80.

    Google Scholar 

  28. Partridge EE, Shingleton HM, Menck HR. The national cancer data base report on endometrial cancer. J Surg Oncol. 1996;61(2):111–23.

    Article  CAS  Google Scholar 

  29. ASTEC Study Group, Kitchener H, Swart AM, Qian Q, et al. Efficacy of systematic pelvic lymphadenectomy in endometrial cancer (MRC ASTEC trial): a randomised study. Lancet. 2009;373(9658):125–36.

    Article  Google Scholar 

  30. Rossi EC, Kowalski LD, Scalici J, et al. A comparison of sentinel lymph node biopsy to lymphadenectomy for endometrial cancer staging (FIRES trial): a multicentre, prospective, cohort study. Lancet Oncol. 2017;18(3):384–92.

    Google Scholar 

  31. Tan J, Chetty N, Kondalsamy-Chennakesavan S, et al. Validation of the FIGO 2009 staging system for carcinoma of the vulva. Int J Gynecol Cancer. 2012;22(3):498–502.

    Google Scholar 

  32. Collarino A, Donswijk ML, van Driel WJ, et al. The use of SPECT/CT for anatomical mapping of lymphatic drainage in vulvar cancer: possible implications for the extent of inguinal lymph node dissection. Eur J Nucl Med Mol Imaging. 2015;42(13):2064–71.

    Google Scholar 

  33. Altgassen C, Hertel H, Brandstädt A, et al. Multicenter validation study of the sentinel lymph node concept in cervical cancer: AGO Study Group. J Clin Oncol. 2008;26(18):2943–51.

    Google Scholar 

  34. Klapdor R, Länger F, Gratz KF, et al. SPECT/CT for SLN dissection in vulvar cancer: improved SLN detection and dissection by preoperative three-dimensional anatomical localisation. Gynecol Oncol. 2015;138(3):590–6.

    Google Scholar 

  35. Beneder C, Fuechsel FG, Krause T, et al. The role of 3D fusion imaging in sentinel lymphadenectomy for vulvar cancer. Gynecol Oncol. 2008;109(1):76–80.

    Google Scholar 

  36. Martínez A, Zerdoud S, Mery E, et al. Hybrid imaging by SPECT/CT for sentinel lymph node detection in patients with cancer of the uterine cervix. Gynecol Oncol. 2010;119(3):431–5.

    Google Scholar 

  37. Pandit-Taskar N, Gemignani ML, Lyall A, et al. Single photon emission computed tomography SPECT-CT improves sentinel node detection and localization in cervical and uterine malignancy. Gynecol Oncol. 2010;117(1):59–64.

    Google Scholar 

  38. Díaz-Feijoo B, Pérez-Benavente MA, Cabrera-Diaz S, et al. Change in clinical management of sentinel lymph node location in early stage cervical cancer: the role of SPECT/CT. Gynecol Oncol. 2011;120(3):353–7.

    Google Scholar 

  39. Kraft O, Havel M. Detection of sentinel lymph nodes in gynecologic tumours by planar scintigraphy and SPECT/CT. Mol Imaging Radionucl Ther. 2012;21(2):47–55.

    Article  Google Scholar 

  40. Belhocine TZ, Prefontaine M, Lanvin D, et al. Added-value of SPECT/CT to lymphatic mapping and sentinel lymphadenectomy in gynaecological cancers. Am J Nucl Med Mol Imaging. 2013;3(2):182–93.

    Google Scholar 

  41. Collarino A, Perotti G, Giordano A. Pitfall detected by SPECT/CT in vulvar cancer sentinel lymph node mapping. Case reports. In: Herrmann K, Nieweg OE, Povoski SP, Stephen P, editors. Radioguided current applications and innovative directions in clinical practice. Basel: Springer; 2016. p. 483–94.

    Google Scholar 

  42. Garganese G, Bove S, Zagaria L, et al. Ultrasound and 3D SPECT/CT fusion to identify sentinel lymph nodes in vulvar cancer: a feasibility study. Ultrasound Obstet Gynecol. 2019;54(4):545–51. https://doi.org/10.1002/uog.20364. [Epub ahead of print].

  43. Sinno AK, Fader AN, Roche KL, et al. A comparison of colorimetric versus fluorometric sentinel lymph node mapping during robotic surgery for endometrial cancer. Gynecol Oncol. 2014;134(2):281–6.

    Article  Google Scholar 

  44. de Hullu JA, Oonk MH, Ansink AC, et al. Pitfalls in the sentinel lymph node procedure in vulvar cancer. Gynecol Oncol. 2004;94(1):10–5.

    Article  Google Scholar 

  45. Fons G, ter Rahe B, Sloof G, et al. Failure in the detection of the sentinel lymph node with a combined technique of radioactive tracer and blue dye in a patient with cancer of the vulva and a single positive lymph node. Gynecol Oncol. 2004;92(3):981–4.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This chapter is a revision of the original chapter written by P. Paredes and S. Vidal-Sicart in the previous edition of the book.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Angela Collarino .

Editor information

Editors and Affiliations

Clinical Cases

Clinical Cases

Case 14.1 SLN Mapping in Vulvar Carcinoma: False-Positive Finding Due to Lymphatic Duct

Alberto Fragano Danilo Fortini Luca Zagaria

Background Clinical Case

A 73-year-old woman with two foci of invasive vulvar squamous cell carcinoma located in both left and right labia minora. She was scheduled for radical vulvectomy and bilateral SLNB.

Lymphoscintigraphy

Fig. 14.6
figure 6

After the application of local anesthesia, 99mTc-nanocolloid (four aliquots of 74 MBq in 0.2 mL) was injected around the two lesions the day before the surgery (2-day protocol). The anterior dynamic (a) and early (b) images show unilateral lymphatic drainage with visualization of two SLNs (arrows, b) in the left groin. The anterior late image (c) shows bilateral lymphatic drainage with only one SLN (arrow) in the left groin corresponding to a single focal uptake (yellow arrow) on transaxial SPECT/CT image (d) and a non-enlarged lymph node (yellow arrow) located in the medial superior inguinal zone on transaxial low-dose CT (e). In conclusion, the two foci of uptake defined as SLNs in the left groin at dynamic and early planar images correspond to one SLN and to its lymphatic vessel on transaxial fused SPECT/CT image, respectively

Case 14.2 SLN Mapping in Vulvar Carcinoma: Visualization of Pelvic SLN

Alberto Fragano Danilo Fortini Germano Perotti

Background Clinical Case

An 82-year-old woman who had a vulvar squamous cell carcinoma of clitoris. She was scheduled for radical vulvectomy and bilateral SLNB.

Lymphoscintigraphy

Fig. 14.7
figure 7

After the application of local anesthesia, 99mTc-nanocolloid (four aliquots of 37 MBq in 0.1 mL) was injected around the tumor the same day of the surgery (1-day protocol). The anterior dynamic images (a) show bilateral lymphatic drainage with one SLN in the right groin (arrow) corresponding to one focal uptake (red arrow) on transaxial SPECT/CT image (b) and non-enlarged lymph node (red arrow) in the medial superior zone on transaxial low-dose CT (c), plus another focal uptake in the pelvic area (yellow dashed arrow, d) corresponding to a non-enlarged lymph node (yellow dashed arrow) located in the external iliac zone on transaxial low-dose CT (e)

Case 14.3 SLN Mapping in Cervical Cancer: Visualization of Para-aortic SLN

Sergi Vidal-Sicart Andrés Perissinotti Sebastian Casanueva

Background Clinical Case

A 34-year-old woman who had early-stage cervical cancer (stage IB1).

Lymphoscintigraphy

Fig. 14.8
figure 8

After peritumoral injection of 111 MBq of ICG-99mTc-nanocolloid in four deposits of 0.5 mL each (a), anterior planar images were obtained at 30 min (early imaging, b) and 120 min (late imaging, c). A focal uptake in the para-aortic area (red arrow) was clearly seen in the early image (b), and was considered as para-aortic SLN. Coronal CT image with 3D volume rendering (d) shows the depicted SLN with the surrounding anatomical structures. It is unusual to find para-aortic SLNs after radiotracer injection into the uterine cervix. Para-aortic nodal spread occurs usually orderly, with progressive involvement of the pelvic and common iliac lymph nodes before para-aortic lymph nodes. However, cervical cancer can occasionally metastasize directly to the para-aortic lymph nodes by embolization of the posterior lymphatic pathway (presacral area). Just before surgery, 2 mL of methylene blue dye was injected in the same site as the radiotracer. During laparoscopy (e), a net of blue-stained lymphatic channels (blue arrows) were depicted running upwards to the para-aortic SLN. This SLN was excised and exhibited radioactivity (150 cps/s), fluorescence (f), and blue color. Histopathology did not show metastatic involvement in this, nor in two additional SLNs located in the pelvis

Case 14.4 SLN Mapping in Endometrial Cancer

Sergi Vidal-Sicart Andrés Tapias Sebastian Casanueva

Background Clinical Case

A 70-year-old woman who had endometrial carcinoma with myometrial involvement >50% of the uterine wall thickness.

Lymphoscintigraphy

Fig. 14.9
figure 9

After injection of 185 MBq of hybrid tracer (ICG-99mTc-nanocolloid) in the myometrial tissue guided by transvaginal ultrasound, early (at 30 min, a) and late (at 120 min, b) images were obtained. The deep injection in the myometrial area results in fast diffusion into the bloodstream with ensuing early visualization of the bone marrow that can hinder visualization of lymph nodes. Only one area of focal uptake in the right pelvic area was seen at early (a) and late (b) planar imaging, and was considered as a pelvic SLN. Coronal CT images with 3D volume rendering (c) and their corresponding transaxial CT images (d, e) show a second focal uptake in the left pelvic side (red arrow, d) corresponding to a second SLN in the left obturator fossae. During surgery, only the left SLN was resected. No activity was observed with the laparoscopic adapted gamma probe nor fluorescence was detected in the right pelvic area. Histopathology revealed metastasis of the resected left SLN. Pelvic lymphadenectomy resulted in harvesting of 12 negative lymph nodes and 1 positive node in the left side, and only 5 negative lymph nodes in the right pelvis

Rights and permissions

Reprints and permissions

Copyright information

© 2020 Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Collarino, A., Zurru, A., Vidal-Sicart, S. (2020). Preoperative and Intraoperative Lymphatic Mapping for Radioguided Sentinel Node Biopsy in Cancers of the Female Reproductive System. In: Mariani, G., Vidal-Sicart, S., Valdés Olmos, R. (eds) Atlas of Lymphoscintigraphy and Sentinel Node Mapping. Springer, Cham. https://doi.org/10.1007/978-3-030-45296-4_14

Download citation

  • DOI: https://doi.org/10.1007/978-3-030-45296-4_14

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-45295-7

  • Online ISBN: 978-3-030-45296-4

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics